Reaktion #1988

ord-eb07eb00507a464db46f471df4d8364d

Reaktionsgleichung

O=C([O-])[O-].[K+].[K+]
K2CO3
O=C1CC2CN(Cc3ccccc3)CC2C(=O)N1
compound
O=C1CC2CN(Cc3ccccc3)CC2C(=O)N1
2-benzyl-4,6-dioxooctahydropyrrolo[3.4-c]pyridine
BrCc1ccccc1
benzyl bromide
O=C1CC2CN(Cc3ccccc3)CC2C(=O)N1Cc1ccccc1
title compound
Ausbeute 111.4%
O=C1CC2CN(Cc3ccccc3)CC2C(=O)N1Cc1ccccc1
2,5-dibenzyl-4,6-dioxooctahydropyrrolo[3.4-c]pyridine
Ausbeute 111.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwas washed with water and brine
  2. 2
    Sonstigedried
  3. 3
    Einengenconcentrated

Vorschrift

To a mixture of 905 mg of K2CO3 and 400 mg of the compound from step 457b in 5 mL of DMF was added 308 mg of benzyl bromide, and the reaction mixture was stirred at room temperature under N2 for 6.5 hours. The mixture was diluted with ethyl acetate, which was washed with water and brine, dried and concentrated to give 610 mg of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726182uspto-grants-1998_03